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88245-74-3

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88245-74-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88245-74-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,4 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88245-74:
(7*8)+(6*8)+(5*2)+(4*4)+(3*5)+(2*7)+(1*4)=163
163 % 10 = 3
So 88245-74-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H12/c1-5-8(4)6-7(2)3/h1,6-7H,2-4H3/b8-6+

88245-74-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dimethylhex-3-en-1-yne

1.2 Other means of identification

Product number -
Other names 3,5-Dimethyl-3-hexen-1-yne

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:88245-74-3 SDS

88245-74-3Upstream product

88245-74-3Downstream Products

88245-74-3Relevant articles and documents

Isomerization of propargylic alcohols into α,β-unsaturated carbonyl compounds catalyzed by the sixteen-electron allyl-ruthenium(II) complex [Ru(η3-2-C3H4Me)(CO)(dppf)] [SbF 6]

Cadierno, Victorio,Garcia-Garrido, Sergio E.,Gimeno, Jose

, p. 101 - 110 (2007/10/03)

The 16-e- (η3-allyl)-ruthenium(II) complex [Ru(η3-2-C3H4Me)(CO)(dppf)][SbF 6] is an efficient catalyst for the regioselective isomerization of terminal propargylic alcohols HC≡CCR1R2(OH) into α,β-unsaturated aldehydes R1R2C=CHCHO or ketones R3R4C=C(R1)COMe (if R2 = CHR3R4) under mild conditions. This complex has been also used as catalyst for the preparation of conjugated 1,3-enynes via dehydration of propargylic alcohols.

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